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Genome Medicine|February 26, 2021
Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephalyWilliam L Macken, Annie Godwin, Gabrielle Wheway, et al.American Journal of Medical Genetics. Part A|February 19, 2015
Expanding the genetic and phenotypic spectrum of popliteal pterygium disordersElizabeth J Leslie, James O'Sullivan, Michael L Cunningham, et al.BMC Medical Genomics|July 19, 2020
What is the right sequencing approach? Solo VS extended family analysis in consanguineous populationsAhmed Alfares, Lamia Alsubaie, Taghrid Aloraini, et al.European Journal of Human Genetics : EJHG|October 7, 2018
The Global State of the Genetic Counseling ProfessionMaryAnn Abacan, Lamia Alsubaie, Kristine Barlow-Stewart, et al.Pageof 2